| Human Disease |
Neuronopathy, Distal Hereditary Motor, Type Viia; HMN7A OMIM ID: 158580 |
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| Synonyms | Dhmn7a; DHMNVP; Harper-Young Myopathy; Hmn Viia; Neuropathy, Distal Hereditary Motor, Type Viia; Spinal Muscular Atrophy, Distal, with Vocal Cord Paralysis | |||||||||||||||||||||
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Genes and mouse models |
Mutations in human and/or mouse homologs are associated with this disease
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Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc |
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last database update 06/05/2013 MGI 5.13 |
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